(Q41586869)

4 October 2017

1 reference

title

Functional methionine synthase deficiency due to cblG disorder: a report of two patients and a review (English)

1 reference

methylcobalamin deficiency type cblG

4 October 2017

Arakawa's syndrome II

1 reference

based on heuristic

inferred from title

1 reference

Harding CO

1

1 reference

4 October 2017

Arnold G

2

1 reference

4 October 2017

Barness LA

3

1 reference

4 October 2017

Wolff JA

4

1 reference

4 October 2017

Rosenblatt DS

5

1 reference

4 October 2017

1 September 1997

1 reference

American Journal of Medical Genetics Part A

4 October 2017

1 reference

4 October 2017

71

1 reference

4 October 2017

4

1 reference

4 October 2017

384-390

1 reference

Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthood

4 October 2017

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970905%2971%3A4%3C384%3A%3AAID-AJMG3%3E3.0.CO%3B2-U

Inherited defects of vitamin B12 metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970905%2971%3A4%3C384%3A%3AAID-AJMG3%3E3.0.CO%3B2-U

Defects in human methionine synthase in cblG patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970905%2971%3A4%3C384%3A%3AAID-AJMG3%3E3.0.CO%3B2-U

Interrelations of vitamin B12 and folic acid metabolism: folic acid clearance studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970905%2971%3A4%3C384%3A%3AAID-AJMG3%3E3.0.CO%3B2-U

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970905%2971%3A4%3C384%3A%3AAID-AJMG3%3E3.0.CO%3B2-U

Altered vitamin B12 metabolism in fibroblasts from a patient with megaloblastic anemia and homocystinuria due to a new defect in methionine biosynthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970905%2971%3A4%3C384%3A%3AAID-AJMG3%3E3.0.CO%3B2-U

Prenatal vitamin B12 therapy of a fetus with methylcobalamin deficiency (cobalamin E disease).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970905%2971%3A4%3C384%3A%3AAID-AJMG3%3E3.0.CO%3B2-U

Vitamin B12 responsive homocystinuria and megaloblastic anemia: heterogeneity in methylcobalamin deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970905%2971%3A4%3C384%3A%3AAID-AJMG3%3E3.0.CO%3B2-U

Genetic heterogeneity among patients with methylcobalamin deficiency. Definition of two complementation groups, cblE and cblG.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970905%2971%3A4%3C384%3A%3AAID-AJMG3%3E3.0.CO%3B2-U

Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970905%2971%3A4%3C384%3A%3AAID-AJMG3%3E3.0.CO%3B2-U

10.1002/(SICI)1096-8628(19970905)71:4<384::AID-AJMG3>3.0.CO;2-U

21 January 2018

Identifiers

DOI

1 reference

4 October 2017

1 reference